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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
1981-9-15
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pubmed:abstractText |
The synthesis of a set of protected ribonucleosides bearing a 5'-monomethoxytrityl group and a 2'-t-butyldimethylsilyl group (series 1, MMTNSiOH) and another set having a 2'-t-butyldimethylsilyl and a 3'-levulinyl group (series 3, HONSiLV) is described. These two sets of derivatives along with the dichlorophosphite condensation procedure lead to a rapid and versatile synthetic procedure for the preparation of oligoribonucleotides. Nucleotide chains possessing a methoxytrityl group at the 5'-end and a levulynyl group at the 3'-end possess an easily detected PMR label at each end (a distinct methyl singlet). The synthetic method is illustrated by the synthesis of a hexadecauridylic acid by a block condensation procedure.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Indicators and Reagents,
http://linkedlifedata.com/resource/pubmed/chemical/Oligonucleotides,
http://linkedlifedata.com/resource/pubmed/chemical/Oligoribonucleotides,
http://linkedlifedata.com/resource/pubmed/chemical/Silicon,
http://linkedlifedata.com/resource/pubmed/chemical/Trityl Compounds
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pubmed:status |
MEDLINE
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pubmed:issn |
0261-3166
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
147-50
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading | |
pubmed:year |
1980
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pubmed:articleTitle |
A complete procedure for the chemical synthesis of oligoribonucleotides.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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